# Predicting complications in emergency department patients with acute coronary syndrome – Existing risk scores versus a new logistic regression model

**Authors:** T. Nilsson, M. Strömfors, A. Trägårdh, A. Mokhtari, A.M. Khoshnood, U. Ekelund

PMC · DOI: 10.1016/j.ahjo.2026.100736 · 2026-02-10

## TL;DR

A new logistic regression model outperforms existing risk scores in predicting complications for acute coronary syndrome patients in emergency departments.

## Contribution

A novel logistic regression model using ED variables provides better complication prediction than established risk scores for ACS patients.

## Key findings

- 7% of acute coronary syndrome patients experienced serious complications.
- The new logistic regression model achieved an AUROC of 0.84, surpassing six existing risk scores.
- Key predictors included age, STEMI, troponin, lactate, shock index, Killip class, and new ECG changes.

## Abstract

Patients with acute coronary syndrome (ACS) are often admitted to monitored wards due to the risk of complications. Several risk prediction scores exist, but their use in the emergency department (ED) is limited. We aimed to compare the ability of existing risk scores with a new logistic regression model in predicting complications in ACS patients.

This was a secondary analysis of data from the ESC TROP trial (NCT03421873), including ACS patients from five EDs in Region Skåne, Sweden (2017–2018). Complications were identified via diagnosis and/or intervention codes and manual chart review. GRACE, GRACE FFE, TIMI, HEART, ACTION ICU, and CHA₂DS₂-VASc scores were calculated. A new logistic regression model was developed, and its predictive performance was assessed using the area under the ROC curve (AUROC) and a net reclassification improvement analysis (NRI).

Among 2223 ACS patients, 164 (7.4%) experienced complications. Independent predictors for complications included age, STEMI, troponin and lactate at arrival, shock index, Killip class, and new ECG changes. The logistic regression model's AUROC 0.84 (95% CI 0.80–0.88) outperformed all known risk scores: GRACE FFE 0.79 (0.75–0.84), ACTION ICU 0.77 (0.72–0.82), GRACE 0.76 (0.70–0.81), TIMI 0.74 (0.68–0.79), HEART 0.69 (0.64–0.74), and CHA₂DS₂-VASc 0.64 (0.59–0.69). Logistic regression improved reclassification of non-events, with a positive non-event NRI compared with all other scores.

Serious complications occurred in 7% of ACS patients. A logistic regression model based on simple ED variables showed excellent predictive performance, surpassing existing risk scores. Improved risk stratification may optimize resource allocation while maintaining patient safety.

Unlabelled Image

•Serious complications occurred in 7% of all ACS patients.•Predictors of complications - age, STEMI, troponin and lactate at arrival, shock index, Killip class, and new ECG changes.•A new logistic regression model demonstrated excellent predictive performance (AUROC 0.84) and outperformed six established risk scores.

Serious complications occurred in 7% of all ACS patients.

Predictors of complications - age, STEMI, troponin and lactate at arrival, shock index, Killip class, and new ECG changes.

A new logistic regression model demonstrated excellent predictive performance (AUROC 0.84) and outperformed six established risk scores.

## Linked entities

- **Diseases:** acute coronary syndrome (MONDO:0005542)

## Full-text entities

- **Genes:** TNNT2 (troponin T2, cardiac type) [NCBI Gene 7139] {aka CMD1D, CMH2, CMPD2, LVNC6, RCM3, TnTC}
- **Diseases:** critically ill (MESH:D016638), shock (MESH:D012769), Complications (MESH:D008107), ACS (MESH:D054058), diabetes mellitus (MESH:D003920), aortic dissection (MESH:D000784), left or right bundle branch block (MESH:D002037), papillary muscle rupture (MESH:D012421), ischemic (MESH:D002545), cardiogenic shock (MESH:D012770), NSTEMI (MESH:D000072658), cardiac arrest (MESH:D006323), pulmonary edema (MESH:D011654), STEMI (MESH:D000072657), malignant arrhythmias (MESH:D001145), ED (MESH:D004630), COPD (MESH:D029424), chest pain (MESH:D002637), left ventricular free wall rupture (MESH:D006341), acute ischemia (MESH:D000208), hypertension (MESH:D006973), Death (MESH:D003643), atrial fibrillation (MESH:D001281), AMI (MESH:D009203), MACE (MESH:D002318), AV-block (MESH:D054537), infarction (MESH:D007238), heart failure (MESH:D006333), hypercholesterolemia (MESH:D006937), depression (MESH:D003866), peripheral artery disease (MESH:D058729), ICD (MESH:D057873), dementia (MESH:D003704), coronary artery disease (MESH:D003324), cardiac (MESH:D006331), VSD (MESH:D000093665), ventricular tachycardia (MESH:D017180), Coronary (MESH:D003323), cardiac tamponade (MESH:D002305), cognitive impairment (MESH:D003072), UA (MESH:D000789)
- **Chemicals:** lactate (MESH:D019344), cardiac troponin T (-), Hs (MESH:D006859), glucose (MESH:D005947), creatinine (MESH:D003404)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12925123/full.md

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Source: https://tomesphere.com/paper/PMC12925123